Shen V, Birchman R, Xu R, Otter M, Wu D, Lindsay R, Dempster D W
Regional Bone Center, Helen Hayes Hospital, W. Haverstraw, New York 10993, USA.
J Clin Invest. 1995 Nov;96(5):2331-8. doi: 10.1172/JCI118289.
Intermittent administration of PTH has been found to be an effective anabolic agent in cancellous bone. We have reported previously that combined treatment with PTH and estrogen in estrogen-deficient rats was beneficial in correcting established osteopenia. To determine if the beneficial effects of PTH therapy can be preserved by estrogen alone and whether PTH therapy can be effective in treating osteopenic subjects stabilized with estrogen, we have undertaken a "crossover" study in the rat model of estrogen-deficiency induced osteopenia. Six-month-old female rats were ovariectomized and after 5 wk treated for 8 wk with vehicle, 30 micrograms/kg per day of rPTH(1-34) plus 15 micrograms/kg per day of 17 beta-estradiol or 17 beta-estradiol alone. One group from each treatment regimen was then sacrificed and for an additional 8 weeks the remaining rats were (a) maintained on their previous treatment; (b) "crossed over" to their reciprocal treatment; or (c) administered vehicle only. At the end of this second 8-wk treatment period all rats were sacrificed. Bone mineral density of the distal femur, histomorphometric measurements of the proximal tibia and mechanical testing of the distal femur and selected vertebral bodies were performed. Our results demonstrated that (a) the gains in bone mass, trabecular connectivity and mechanical strength induced by PTH can be maintained by estrogen alone, but are reversed when both agents are withdrawn; and (b) rats with established osteopenia, maintained on estrogen treatment alone, can derive the full beneficial effects from the addition of PTH to the treatment at a later date. These data indicate that combined and/or sequential use of antiresorptive and anabolic agents may be a promising approach to the treatment of osteoporosis.
间歇性给予甲状旁腺激素(PTH)已被发现是一种有效的松质骨合成代谢剂。我们之前报道过,在雌激素缺乏的大鼠中,PTH与雌激素联合治疗有利于纠正已形成的骨质减少。为了确定单独使用雌激素是否能维持PTH治疗的有益效果,以及PTH治疗对已用雌激素稳定病情的骨质减少患者是否有效,我们在雌激素缺乏诱导的骨质减少大鼠模型中进行了一项“交叉”研究。6月龄雌性大鼠行卵巢切除术,5周后分别用赋形剂、每天30微克/千克的重组人甲状旁腺激素(1-34)加每天15微克/千克的17β-雌二醇或仅用17β-雌二醇治疗8周。然后处死每种治疗方案中的一组大鼠,其余大鼠再额外治疗8周,治疗方式如下:(a)维持之前的治疗;(b)“交叉”接受其对应的治疗;或(c)仅给予赋形剂。在第二个8周治疗期结束时,处死所有大鼠。对股骨远端进行骨密度测量,对胫骨近端进行组织形态计量学测量,并对股骨远端和选定的椎体进行力学测试。我们的结果表明:(a) PTH诱导的骨量增加、小梁连接性和力学强度可单独由雌激素维持,但当两种药物都停用后则会逆转;(b) 已形成骨质减少且仅接受雌激素治疗的大鼠,在后期添加PTH治疗后可获得全部有益效果。这些数据表明,联合和/或序贯使用抗吸收和合成代谢药物可能是治疗骨质疏松症的一种有前景的方法。